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- 저자 : Dae Youn Hwang (검색결과 458 건)
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루프 분할과 종속함수를 이용한 다중첨자 중첩루프의 종속성 제거 기법
박상일,양황규,윤성대 東西大學校 2001 동서논문집 Vol.7 No.-
In this paper, we propose a new method to parallelize multidimensional subscript loop with non-uniform distance. A loop comprise most of the computation in a program and the most important source of parallelism. Multidimensional subscript within a loop difficult to determine for distance to be required loop dependence elimination. Therefore, we propose new methods that used dependency function to eliminate dependence.
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Expression Analysis of the Ligand to Ly-6E.1 Mouse Hematopoietic Stem Cell Antigen
Hwang, Dae-Youn,Min, Dul-Lei,Sonn, Chung-Hee,Chang, Mi-Ra,Lee, Mi-Hyun,Paik, Sang-Gi,Kim, Young-Sang The Korean Society for Integrative Biology 1997 Korean journal of biological sciences Vol.1 No.1
Ly-6E.1 antigen was proposed as a regulatory molecule of T lymphocyte activation, a hematopoietic stem cell marker, a memory cell marker, and an adhesion molecule. Though there were several reports suggesting the presence of Ly-6 ligand, the characterization of the ligand was not yet performed, As an attempt to screen the expression of Ly-6E.1 ligand, we prepared a probe for detecting Ly-6E.1 ligand by producing a fusion protein between Ly-6E.1 and $hlgC_{r1}$, A mammalian cell expression vector with Ly-6E.$1/hlgC_{r1}$ chimeric cDNA was transfected in SP2/0-Ag14 myeloma cells, and stable transfectants were selected. The fusion protein was produced as a dimer and maintained the epitopes for monoclonal antibodies specific for Ly-6E.1 and for anti-human lgG antibody. The purified fusion protein through Gammabind G column was used for FACS analyses for the expression of Ly-6E.1 ligand. The fusion protein interacted with several cell lines originating from B cells, T cells, or monocytes. The fusion Protein also strongly stained bone marrow, lymph node, and spleen cells, but thymic cells weakly, if any. The staining was more obvious in C57BL/6 $(Ly-6^b)$ than Balb/c $(Ly-6^a)$ mice. These results suggest that the interaction of Ly-6E.1 with Ly-6E.1 ligand may function both in the stem cell environment and in the activation of mature lymphocytes. The fusion protein may be a valuable tool in characterization of biochemical properties of the Ly-6E.1 ligand and, further, in isolating its cDNA.
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Expression Analysis of the Ligand to Ly-6E.1 Mouse Hematopoietic Stem Cell Antigen
Hwang, Dae Youn,Min, Dullei,Sonn, Chung Hee,Chang, Mi Ra,Lee, Mi Hyun,Paik, Sang-Gi,Kim, Young Sang 충남대학교 생물공학연구소 1998 생물공학연구지 Vol.6 No.-
Ly-6E.1 antigen was proposed as a regulatory molecule of T lymphocyte activation, a hematopoietic stem cell marker, a memory cell marker, and an adhesion molecule. Though there were several reports suggesting the presence of Ly-6 ligand, the characterization of the ligand was not yet performed. As an attempt to screen the expression of Ly-6E.1 ligand, we prepared a probe for detecting Ly-6E.1 ligand by producing a fusion protein between Ly-6E.1 and hlgC_r1. A mammalian cell expression vector with Ly-6E.1/hlgC_r1 chimeric cDNA was transfected in SP2/0-Ag14 myeloma cells, and stable transfectants were selected. The fusion protein was produced as a dimer and maintained the epitopes for monoclonal antibodies specific for Ly-6E.1 and for anti-human lgG antibody. The purified fusion protein through Gammabind G column was used for FACS analyses for the expression of Ly-6E.1 ligand. The fusion protein interacted with several cell lines originating from B cells, T cells, or monocytes. The fusion protein also strongly stained bone marrow, lymph node, and spleen cells, but thymic cells weakly, if any. The staining was more obvious in C57BL/6 (Ly-6^b) than Balb/c (Ly-6^a) mice. These results suggest that the interaction of Ly-6E.1 with Ly-6E.1 ligand may function both in the stem cell environment and in the activation of mature lymphocytes. The fusion protein may be a valuable tool in characterization of biochemical properties of the Ly-6E.1 ligand and, further, in isolating its cDNA.
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